Package 79903-232-90

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 79903-232-90
Digits Only 7990323290
Product NDC 79903-232
Product ID 79903-232_9641a476-de98-47f1-b608-d687aaba9e42
Description

1 BOTTLE in 1 CARTON (79903-232-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-14
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9641a476-de98-47f1-b608-d687aaba9e42", "openfda": {"upc": ["0194346189090"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["1292c0ca-343e-adcc-e063-6394a90ab9fa"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-232-90)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79903-232-90", "marketing_start_date": "20240214"}], "brand_name": "Naproxen Sodium", "product_id": "79903-232_9641a476-de98-47f1-b608-d687aaba9e42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-232", "generic_name": "Naproxen Sodium", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20240214", "listing_expiration_date": "20261231"}